| ²é¿´: 486 | »Ø¸´: 2 | ||
¶ªÊ§µÄС¹ÇÍ·½ð³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| ̼Æ×Êý¾ÝÈçÏÂ37.461,39.671,50.748,50.953,54.620,60.036,68.464,69.421,70.591,114.531,123.798,128.564,132.786,132.916,137.509,140.282,141.360,164.919,165.207,166.802 |
» ²ÂÄãϲ»¶
283·Ö²ÄÁÏÓ뻯¹¤Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
349Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
296²ÄÁÏר˶Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸ÉϺ£º£Ñó´óѧ083200ʳƷѧ˶£¬Çóµ÷¼Á£¬½ÓÊÜÆäËûרҵ
ÒѾÓÐ7È˻ظ´
²ÄÁÏ340·Öµ÷¼Á
ÒѾÓÐ8È˻ظ´
316Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
321Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
315Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
330·ÖÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
»¯¹¤µ÷¼Á303·Ö£¬¹ýËļ¶
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬ºÃÐÄÈËÇëÖ¸µãÒ»ÏÂ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
Çó΢Æ×£¬²»Ê¤¸Ð¼¤ÌéÁã
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£¡£¡£¡£¡£¡£¡£¡£¡£¡»¯ºÏÎïCÆ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´

sydong
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 403 (˶ʿ)
- ½ð±Ò: 7797.1
- ºì»¨: 22
- Ìû×Ó: 1800
- ÔÚÏß: 632.4Сʱ
- ³æºÅ: 1255872
- ×¢²á: 2011-04-05
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¶ªÊ§µÄС¹ÇÍ·: ½ð±Ò+20, ·Ç³£¸Ðл 2014-11-19 14:07:13
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¶ªÊ§µÄС¹ÇÍ·: ½ð±Ò+20, ·Ç³£¸Ðл 2014-11-19 14:07:13
|
ÃÀÅ®£¬¸ñʽ´íÎó°¡£¡£¡2λСÊý¾Í¿ÉÒÔÁ˰¡£¡£¡²éѯ½á¹û£º¹²²éµ½60¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . vernodalol ÏàËÆ¶È:100% Pharmaceutical Biology 2007 45 195-199 Antioxidant Constituents in Vernonia amygdalina. Leaves P. Erasto, D.S. Grierson, A.J. Afolayan Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 1 C20H24O8 ÏàËÆ¶È:80% Planta Medica 2003 69 164-166 In Vitro Cytotoxic Elemanolides from Vernonia lasiopus J.L.Koul,S.Koul,C.Singh,S.C.Taneja,M.Shanmugavel,H.Kampasi,A.K.Saxena,G.N.Qazi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . elescaberin C20H24O7 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2008 10 403-407 A new elemanolide sesquiterpene lactone from Elephantopus scaber Qiao-Li Liang, Zhi-Da Min and Yu-Ping Tang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4,15-Anhydro-4¦Á-hydroxy-15-dihydrocarmanin C20H28O8 ÏàËÆ¶È:55% Phytochemistry 1993 33 1457-1460 Eudesmane and elemane derivatives from Onopordon acaulon Luz Cardona, Alicia Bardon, Begoña Garc¨ªa, Jos¨¦ R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . N-(2-Methoxyethyl)-6-(5-oxo-1-phenylpyrrolidin-3-yl)-2-phenylpyrimidine-5-carboxamide C24H24N4O3 ÏàËÆ¶È:55% Molecules 2012 17 5363-5384 Parallel Synthesis of 2-Substituted 6-(5-Oxo-1-phenylpyrrolidin-3-yl)pyrimidine-5-carboxamides Bojana Črček, Jernej Baškovč, Uroš Grošelj, Drago Kočar, Georg Dahmann, Branko Stanovnik and Jurij Svete Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (2E,2'E)-diisobutyl 3,3'-{5-[(E)-(4-methoxyphenylimino)methyl]thiophene-2,3-diyl}diacrylate C26H31NO5S ÏàËÆ¶È:55% Tetrahedron 2013 69 160-173 Synthesis of functionalized benzothiophenes and dibenzothiophenes by twofold Heck and subsequent 6¦Ð-electrocyclization reactions of 2,3-dibromothiophenes and 2,3-dibromobenzothiophenes Serge-Mith¨¦rand Tengho Toguem, Imran Malik, Munawar Hussain, Jamshed Iqbal, Alexander Villinger, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . N,N'-((14R,19R)-1,32-diazido-13,20-dioxo-3,6,9,24,27,30-hexaoxa-16,17-dithia-12,21-diazadotriacontane-14,19-diyl)bis(4-benzoylbenzamide) C50H60N10O12S2 ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 2014 22 2102-2112 Synthesis and evaluation of effective photoaffinity probe molecule of furospinosulin-1, a hypoxia-selective growth inhibitor Naoyuki Kotoku, Chiaki Nakata, Takashi Kawachi, Takanori Sato, Xiu-Han Guo, Aoi Ito, Yuji Sumii, Masayoshi Arai, Motomasa Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (2E,2'E)-diisobutyl 3,3'-[5-(2-methoxyphenyl)thiophene-2,3-diyl]diacrylate C25H31O5S ÏàËÆ¶È:52.3% Tetrahedron 2013 69 160-173 Synthesis of functionalized benzothiophenes and dibenzothiophenes by twofold Heck and subsequent 6¦Ð-electrocyclization reactions of 2,3-dibromothiophenes and 2,3-dibromobenzothiophenes Serge-Mith¨¦rand Tengho Toguem, Imran Malik, Munawar Hussain, Jamshed Iqbal, Alexander Villinger, Peter Langer Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 1a ÏàËÆ¶È:52.3% Tetrahedron 2013 69 8487-8493 Macrocycles consisting of flexible and rigid segments: enforced folding and host-guest inclusion exciplex formation Xiaomei Tang, Li Lin, Futao Liu, Xiangjun Yue, Bing Gong, Minfeng Li, Lan He Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . dihydroisostrychnine ÏàËÆ¶È:52.3% Organic Magnetic Resonance 1977 9 333-337 Carbon-13 n.m.r. analysis of selected strychnos alkaloids J. Leung and Alan J. Jones Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . pochonin C C18H18Cl2O6 ÏàËÆ¶È:50% Journal of Natural Products 2003 66 829-837 Pochonins A-F, New Antiviral and Antiparasitic Resorcylic Acid Lactones from Pochonia chlamydosporia var. catenulata Veronika Hellwig,Anke Mayer-Bartschmid, Hartwig M¨¹ller, Gisela Greif,Gerald Kleymann,Werner Zitzmann, Hans-Volker Tichy,and Marc Stadler Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Methyl-6-(o-nitro-)benzamidyl-6-deoxy-2,3,4-tri-O-acetyl-¦Á-D-glucopyranoside ÏàËÆ¶È:50% Molecules 2009 14 2447-2457 Synthesis of 3-N-Sugar-substituted-2, 4(1H, 3H)-quinazolinedionesas Anti-Angiogenesis Agents Conghai Huang, Xiangbao Meng, Jingrong Cui and Zhongjun Li Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Methyl-6-(o-nitro-)benzamidyl-6-deoxy-2,3,4-tri-O-acetyl-¦Á-D-mannopyranoside ÏàËÆ¶È:50% Molecules 2009 14 2447-2457 Synthesis of 3-N-Sugar-substituted-2, 4(1H, 3H)-quinazolinedionesas Anti-Angiogenesis Agents Conghai Huang, Xiangbao Meng, Jingrong Cui and Zhongjun Li Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Methyl-6-(N3-)quinazolinedionyl-6-deoxy-2,3,4-tri-O-acetyl-¦Á-D-glucopyranoside ÏàËÆ¶È:50% Molecules 2009 14 2447-2457 Synthesis of 3-N-Sugar-substituted-2, 4(1H, 3H)-quinazolinedionesas Anti-Angiogenesis Agents Conghai Huang, Xiangbao Meng, Jingrong Cui and Zhongjun Li Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . DG-3 dibenzoate C28H28O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1998 46 423-429 Immunosuppressive Components from an Ascomycete, Diplogelasinospora grovesii Haruhiro FUJIMOTO,Junko NAGANO,Kentaro YAMAGUCHI and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 14-Hydroxy-8¦Â-sarracenyloxycostunolide ÏàËÆ¶È:50% Phytochemistry 1996 42 1369-1373 Sesquiterpene lactones from Stevia vaga Luis R. Hern¨¢ndez, C¨¦sar A. N. Catal¨¢n, Carlos M. Cerda-Garc¨ªa-Rojas, Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compund 13 C21H30O7 ÏàËÆ¶È:50% Phytochemistry 1996 41 1113-1117 Sesquiterpene lactones and elemane derivatives from Onopordon myriacanthum Begoña Garc¨ªa, Helen Skaltsa, Francisca I. Navarro, Jos¨¦R. Pedro, Diamando Lazari Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . elemacarmanin ÏàËÆ¶È:50% Phytochemistry 1992 31 3630-3632 Sesquiterpenes, flavonoids and lignans from Onopordon acaulon Luz Cardona, Rafael A. Alemañ, Begoña Garcia, Jos¨¦ R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . elemacarmanin ÏàËÆ¶È:50% Phytochemistry 1989 28 1264-1267 Sesquiterpene lactones and an elemane derivative from Onopordon corymbosum Ma Luz Cardona,Begoña Garcia,Jose R. Pedro,Jorge F. Sinisterra Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 12-methoxy-N(4)-methylakuammicine ÏàËÆ¶È:50% Phytochemistry 1989 28 1241-1244 Alkaloids from Alstonia congensis Catherine Caron,Alain Graftieaux,Georges Massiot,Louisette Le Men-Olivier,Clement Delaude Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 2,4-di(2'-furyl)-2-methyl-1-(2'',3'',5''-tri-o-benzoyl-¦Â-D-ribofuranosyl)-2,3-dihydro-1,5-benzodiazepine ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2010 47 603-610 The facile syntheses of 2,3-dihydro-1H-1,5-benzodiazepines and their ribofuranosides Renuka Jain, Tripti Yadav, Manoj Kumar and Ashok K. Yadav Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . mixture of compound 3a and 4a C36H36O ÏàËÆ¶È:50% Indian Journal of Chemistry Section B 2009 48B 225-230 Synthesis of symmetrical and unsymmetrical trisubstituted benzene derivatives through ring-closing alkyne metathesis strategy and Kotha,Sambasivarao; Bansal,Deepti; Kumar,Ramanatham Vinod Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 5-methoxycarbonyl-6-hydroxy-6-methyl-4-(p-methoxyphenyl)-4,5,6,7-tetrahydro-3-hydroxy-2-(2-pyridinyl)indazole C22H23N3O5 ÏàËÆ¶È:50% Heterocycles 2008 75 537-554 A Facile Synthesis of 4-Aryl-5-alkoxycarbonyl-6-hydroxy-6-methyl-4, 5, 6, 7-tetrahydro-3-hydroxy-2-(pyridin-2-yl)indazoles and Their NMR Characterizations Shanmugasundaram Amirthaganesan, Gopalakrishnan Aridoss, Young Hwan Park, Jong Su Kim, Se Mo son, and Yeon Tae Jeong Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . gliocladride C22H30N2O3 ÏàËÆ¶È:50% Pharmazie 2007 62 478-479 A new piperazine-2,5-dione from the marine fungus Gliocladium sp. Yao Yao, Li Tian, Jia-Qing Cao and Yue-Hu Pei Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 8e C18H14F3N2O6 ÏàËÆ¶È:50% Tetrahedron Letters 2005 46 201-203 The multicomponent reaction of dimethoxycarbene, dimethyl butynedioate and electrophilic styrenes: an unprecedented synthesis of highly substituted cyclopentenone acetals Vijay Nair, P.B. Beneesh, V. Sreekumar, S. Bindu, Rajeev S. Menon, Ani Deepthi Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 39a ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1998 6 1185-1208 Design, synthesis and biological evaluation of nonpeptide integrin antagonists K.C. Nicolaou, John I. Trujillo, Bernd Jandeleit, Kelly Chibale, M. Rosenfeld, B. Diefenbach, D.A. Cheresh, S.L. Goodman Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 1-Phenylmethyl-4-[¦Á,a-diphenyl-(1-tricyclo[3.3.1.13,7]-decyl)methyl]piperazine C33H38N2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 3323-3331 Synthesis, ¦Ò1, ¦Ò2-receptors binding affinity and antiproliferative action of new C1-substituted adamantanes Stefanos Riganas, Ioannis Papanastasiou, George B. Foscolos, Andrew Tsotinis, Jean-Jacques Bourguignon, Guillaume Serin, Jean-François Mirjolet, Kostas Dimas, Vassilios N. Kourafalos, Andreas Eleutheriades, Vassilios I. Moutsos, Humaira Khan, Stavroula Ge Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 8-O-(2-methoxymethyl-2-propenoyl)-3-hydroxy-4(15),10(14),11(13)-guaiatrien-12,6-olide C20H24O6 ÏàËÆ¶È:50% Heterocycles 2002 57 151-155 New Guaiane-Type Sesquiterpene Lactones from Hemisteptia lyrata Bunge Tae Joung Ha, Min Suk Yang, Yunbae Pak, Jong Rok Lee, Kyung Dong Lee, Hwan Mook Kim, and Ki Hun Park* Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 3-(2-(allylmethylamino)ethyl)-3-(4-chlorophenyl)isochroman-1-one oxalate C23H24ClNO6 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 4844-4854 Optimization of isochromanone based urotensin II receptor agonists Fredrik Lehmann, Erika A. Currier, Roger Olsson, Jian-Nong Ma, Ethan S. Burstein, Uli Hacksell, Kristina Luthman Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (2R,4S)-4-[(3-bromophenylsulfanyl)methyl]-2-[2-(4-chlorophenyl)ethyl]-2-[(1H-imidazol-1-yl)methyl]-1,3-dioxolane hydrochloride C22H23BrCl2N2O2S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2009 17 2461-2475 Synthesis and evaluation of imidazole¨Cdioxolane compounds as selective heme oxygenase inhibitors: Effect of substituents at the 4-position of the dioxolane ring Jason Z. Vlahakis, Maaike Hum, Mona N. Rahman, Zongchao Jia, Kanji Nakatsu, Walter A. Szarek Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . butyl 4-chloro-2-(2-bromobenzamido)benzoate C18H17BrClNO3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 5803-5814 Synthesis and anti-platelet evaluation of 2-benzoylaminobenzoate analogs Pei-Wen Hsieh, Shin-Zan Chiang, Chin-Chung Wu, Yi-Ching Lo, Yu-Tzu Shih, Yang-Chang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . izuminoside C C20H18N2O8 ÏàËÆ¶È:50% The Journal of Antibiotics 2011 64 271-275 Isolation and structure elucidation of izuminosides A¨CC: a rare phenazine glycosides from Streptomyces sp. IFM 11260 Mohamed S Abdelfattah, Kazufumi Toume and Masami Ishibashi Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . synerazol C22H23NO7 ÏàËÆ¶È:50% The Journal of Antibiotics 1991 44 382-389 SYNERAZOL, A NEW ANTIFUNGAL ANTIBIOTIC OSAMU ANDO, HITOMI SATAKE, MUTSUO NAKAJIMA, AKIRA SATO, TAKEMICHI NAKAMURA, TAKESHI KINOSHITA, KOUHEI FURUYA, TATSUO HANEISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . Ph3bNOH C38H46N2O6 ÏàËÆ¶È:50% Tetrahedron 2012 68 6193-6197 Polyether-bridged bis(tert-butyl nitroxide) paramagnetic hosts showing receptor ability to calcium(II) and barium(II) ions Sayaka Osada, Naoki Hirosawa, Takayuki Ishida Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (3Z,4E)-ethyl 9-bromo-7-chloro-3-(2-ethoxy-2-oxoethylidene)-2,3-dihydrobenzooxepine-4-carboxylate ÏàËÆ¶È:50% Tetrahedron 2012 68 6289-6297 Wittig homologation of 2-(chloromethyl)-2H-chromen-2-ol derivatives: a new facile synthesis of substituted 2,3-dihydrobenzoxepine-4-carboxylates Bhimapaka China Raju, Gannerla Saidachary, Jaladi Ashok Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . N-[2-(2-allyl-3,4-dimethoxyphenyl)-1-methylethyl]benzenesulfonamide C20H25NO4S ÏàËÆ¶È:50% Tetrahedron 2012 68 10272-10279 Synthesis of tetrahydro-3-benzazepines Meng-Yang Chang, Chieh-Kai Chan, Shin-Ying Lin, Ru-Ting Hsu Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . N-[2-[bis(4-fluorophenyl)methoxy]ethyl]-N'-[3-(4-bromophenyl)-2-propenyl]-1,2-ethanediamine C28H27N2O6F2Br ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1999 42 3647-3656 Design, Synthesis, and Biological Evaluation of Novel Non-Piperazine Analogues of 1-[2-(Diphenylmethoxy)ethyl]- and 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazines as Dopamine Transporter Inhibitors Sung-Woon Choi, David R. Elmaleh, Robert N. Hanson, and Alan J. Fischman Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . trans-N-tert-butyl-2-(3-azido-2-oxo-5-cyclohexyl-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)ethanoic acid amide C22H31N5O2 ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1994 37 3789-3811 5-Phenyl-3-ureidobenzazepin-2-ones as Cholecystokinin-B Receptor Antagonists John A. Lowe III, David L. Hageman, Susan E. Drozda, Stafford McLean, Dianne K. Bryce, Rosemary T. Crawford, Stevin Zorn, Jean Morrone, Jon Bordner Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . cis-N-tert-butyl-2-(3-amino-2-oxo-5-cyclohexyl-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)ethanoic acid amide C22H33N3O2 ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1994 37 3789-3811 5-Phenyl-3-ureidobenzazepin-2-ones as Cholecystokinin-B Receptor Antagonists John A. Lowe III, David L. Hageman, Susan E. Drozda, Stafford McLean, Dianne K. Bryce, Rosemary T. Crawford, Stevin Zorn, Jean Morrone, Jon Bordner Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . (Z)-2-(4-((2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)-N-(4-methoxyphenyl)acetamide ÏàËÆ¶È:50% Archiv der Pharmazie 2012 345 517-524 Synthesis and Evaluation of 5-Benzylidenethiazolidine-2,4-dione Derivatives for the Treatment of Non-Alcoholic Fatty Liver Disease Liang Ma, Jinying Chen, Xiaolin Liang, Caifei Xie, Chongyang Deng, Li Huang, Aihua Peng, Yuanquan Wei and Lijuan Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . solphenazine E C20H20N2O7 ÏàËÆ¶È:50% Journal of Natural Products 2013 76 91-96 Solphenazines A¨CF, Glycosylated Phenazines from Streptomyces sp. Strain DL-93 Yudi Rusman, Lisa M. Oppegard, Hiroshi Hiasa, Christopher Gelbmann, and Christine E. Salomon Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . 2-[2-phenyl-1-(2-benzyl-1,3,4-oxadiazol-5-yl)ethyl]-1,2-benzisothiazol-3(2H)-3-one C24H19N3O2S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2013 21 102-113 Design, synthesis and characterization of novel 1,2-benzisothiazol-3(2H)-one and 1,3,4-oxadiazole hybrid derivatives: Potent inhibitors of Dengue and West Nile virus NS2B/NS3 proteases Huiguo Lai, Dengfeng Dou, Sridhar Aravapalli, Tadahisa Teramoto, Gerald H. Lushington, Tom M. Mwania, Kevin R. Alliston, David M. Eichhorn, Radhakrishnan Padmanabhan, William C. Groutas Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 2-[2-phenyl-1-(2-p-cyanophenyl-1,3,4-oxadiazol-5-yl)ethyl]-1,2-benzisothiazol-3(2H)-one C24H16N4O2S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2013 21 102-113 Design, synthesis and characterization of novel 1,2-benzisothiazol-3(2H)-one and 1,3,4-oxadiazole hybrid derivatives: Potent inhibitors of Dengue and West Nile virus NS2B/NS3 proteases Huiguo Lai, Dengfeng Dou, Sridhar Aravapalli, Tadahisa Teramoto, Gerald H. Lushington, Tom M. Mwania, Kevin R. Alliston, David M. Eichhorn, Radhakrishnan Padmanabhan, William C. Groutas Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 2-[2-phenyl-1-(2-p-methoxyphenyl-1,3,4-oxadiazol-5-yl)ethyl]-1,2-benzisothiazol-3(2H)-one C24H19N3O3S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2013 21 102-113 Design, synthesis and characterization of novel 1,2-benzisothiazol-3(2H)-one and 1,3,4-oxadiazole hybrid derivatives: Potent inhibitors of Dengue and West Nile virus NS2B/NS3 proteases Huiguo Lai, Dengfeng Dou, Sridhar Aravapalli, Tadahisa Teramoto, Gerald H. Lushington, Tom M. Mwania, Kevin R. Alliston, David M. Eichhorn, Radhakrishnan Padmanabhan, William C. Groutas Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 4-(4-chlorobenzoyl)-6-ethoxycarbonyl-1-ethyl-3,4-dihydro-2(1H)-quinolinone C21H20ClNO4 ÏàËÆ¶È:50% Tetrahedron 2013 69 3293-3301 Free radical cyclization reactions of allylsulfonyl substituted N-aryl amide derivatives Che-Ping Chuang, An-I Tsai, Ming-Yi Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . N-tert-butyl-4,5-dihydro-5-(5-fluoro-2-nitrophenyl)-1,2,3-triazolo[1,5-a][1,4]benzodiazepine-6-carboxamide C21H21FN6O3 ÏàËÆ¶È:50% Tetrahedron 2013 69 3506-3510 Synthesis of novel fused 4,5-dihydro-1,2,3-triazolo[1,5-a][1,4]benzodiazepine derivatives via four-component Ugi¨CSmiles-type reaction Mina Saeedi, Mohammad Mahdavi, Alireza Foroumadi, Abbas Shafiee Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . elemacarmanin ÏàËÆ¶È:50% Phytochemistry 2013 95 19-93 Sesquiterpenoids in subtribe Centaureinae (Cass.) Dumort (tribe Cardueae, Asteraceae): Distribution, 13C NMR spectral data and biological properties Review Article Maurizio Bruno, Svetlana Bancheva, Sergio Rosselli, Antonella Maggio Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . ethyl 2-[(2-formyl-3-methyl-1H-indol-1-yl)methyl]-3-(4-methoxyphenyl)prop-2-enoate C23H23NO4 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2013 50 442-449 A Facile One-Pot Synthesis of Pyrrolo[1, 2-a] Indoles by Intramolecular1,3-Dipolar Cycloaddition under Neat-Microwave Irradiation Subramanya Hegde, Jayadevan Jayashankaran, Atanu Ghosal, T.S.R Prasanna, Y. Shivaraj and K. Mohana Raju Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 5-bromo-2-[3-adamantan-1-yl-4-[(2-methoxyethoxy)methoxy]phenyl]-3-methoxypyrazine C25H31BrN2O4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2014 22 1285-1302 Inhibition of I¦ÊB kinase-¦Â and I¦ÊB kinase-¦Á by heterocyclic adamantyl arotinoids Jos¨¦ Garc¨ªa-Rodr¨ªguez, Santiago P¨¦rez-Rodr¨ªguez, Mar¨ªa A. Ortiz, Raquel Pereira, Angel R. de Lera, F. Javier Piedrafita Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . methyl 4-(2-methoxy-2-oxoethyl)-5-(4-methoxyphenyl)-1-phenyl-1H-pyrrole-3-carboxylate ÏàËÆ¶È:50% Tetrahedron 2014 70 2472-2477 An atom-economic synthesis of functionalized pyrroles via a sequential metal-catalyzed three-component reaction Li Yufeng, Shi Jie, Wu Zhengguang, Wang Xinglong, Wu Xiaowei, Gu Jiachao, Bu Hongzhong, Ma Hongfei Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . 2-(4-amino-2-oxopyrimidin-1(2H)-yl)-2-{[(7S)-7,8-dihydro-4H,6H-[1,2,3]triazolo[5,1-c][1,4]oxazepin-7-yl]oxy}ethyl benzoate C19H20N6O5 ÏàËÆ¶È:50% Helvetica Chimica Acta 2014 97 733-743 Synthesis and Anti-HIV Activity of Triazolo-Fused, Medium-Sized Cyclic Nucleoside Analogs Prepared by an Intramolecular Huisgen 1,3-Dipolar Cycloaddition Jingbo Sun, Rongwang Liu, Qiang Fu, Jian Zang, Qiangqiang Tao, Jinchang Wu and Hui Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . 19,20-¦Á-epoxy-15-hydroxyicajine ÏàËÆ¶È:50% Organic Magnetic Resonance 1984 22 345-348 Carbon-13 NMR spectroscopy of some Strychnos alkaloids. Part 2 R. Verpoorte, T. A. van Beek, R. L. M. Riegman, P. J. Hylands and N. G. Bisset Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . 19,20-¦Á-epoxy-15-hydroxyicajine ÏàËÆ¶È:50% Organic Magnetic Resonance 1984 22 345-348 Carbon-13 NMR spectroscopy of some Strychnos alkaloids. Part 2 R. Verpoorte, T. A. van Beek, R. L. M. Riegman, P. J. Hylands and N. G. Bisset Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . compound 6h C20H15Cl3N6O2 ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2010 58 2741-2745 Design, Multicomponent Synthesis, and Bioactivities of Novel Neonicotinoid Analogues with 1,4-Dihydropyridine Scaffold Wenwen Zhang, Xiaobao Yang, Weidong Chen, Xiaoyong Xu, Lu Li, Hongbin Zhai and Zhong Li Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . compound 1 C22H29NO3 ÏàËÆ¶È:50% Journal of the American Chemical Society 1996 118 905-906 Highly Sensitive Colorimetric Detection and Facile Isolation of Diamagnetic Free Radical Adducts of Novel Chromotropic Nitrone Spin Trapping Agents Readily Derived from Guaiazulene David A. Becker Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . SHISEN-1 ÏàËÆ¶È:50% Chinese Journal of Antibiotics 1998 23 107-109 SHISEN-1, a novel phenazine antibiotic from Strep toplanospora viridis ¢ò. Physico-chemical properties and structure elucidation Yue, Hongfei, and, Chen, Yongle, Koko, Sugawara Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . [1-Oxo-6-(4-piperidinium-4-yl-benzoylamino)-1,3-dihydroisoindol-2-yl]acetic acid trifluoroacetate C22H23N3O4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2013 21 4646-4661 Synthesis, biological evaluation, X-ray molecular structure and molecular docking studies of RGD mimetics containing 6-amino-2,3-dihydroisoindolin-1-one fragment as ligands of integrin ¦ÁIIb¦Â3 Andrei A. Krysko, Georgiy V. Samoylenko, Pavel G. Polishchuk, Marina S. Fonari, Victor Ch. Kravtsov, Sergei A. Andronati, Tatyana A. Kabanova, Janusz Lipkowski, Tetiana M. Khristova, Victor E. Kuz¡¯min, Vladimir M. Kabanov, Olga L. Krysko, Alexandre A. Var Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . (R)-Benzyl3-(4-(3,5-Dibromobenzyloxy)-phenylsulfonamido)-4-(hydroxyamino)-4-oxobutylcarbamate C25H25Br2N3O7S ÏàËÆ¶È:50% Journal of Medicinal Chemistry 2013 56 8089-8103 Selective Arylsulfonamide Inhibitors of ADAM-17: Hit Optimization and Activity in Ovarian Cancer Cell Models Elisa Nuti, Francesca Casalini, Salvatore Santamaria, Marina Fabbi, Grazia Carbotti, Silvano Ferrini, Luciana Marinelli, Valeria La Pietra, Ettore Novellino, Caterina Camodeca, Elisabetta Orlandini, Susanna Nencetti, and Armando Rossello Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . Diethyl 2-Ethoxycyclopenta[cd]azulene-1,4-dicarboxylate C20H20O5 ÏàËÆ¶È:50% Helvetica Chimica Acta 2014 97 507-518 A Convenient and Simple Synthesis of Densely Functionalized Cyclopenta[cd]azulenes and Cyclopenta[ef]heptalenes Badugu Devendar, Chien-Kuo Ku, Ling-Yu Cheng, Shu-Juan Yang, Jun-Xiong Chen and Chi-Phi Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . (Z)-ethyl 5-(4-chlorophenyl)-7-methyl-3-oxo-2-(3,4,5-trihydroxybenzylidene)-3,5-dihydro-2H-thiazolo[3,2-a]pyrimidine-6-carboxylate C23H19ClN2O6S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2014 22 4553-4565 Ethyl 2-(benzylidene)-7-methyl-3-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyrimidine-6-carboxylate analogues as a new scaffold for protein kinase casein kinase 2 inhibitorOriginal Research Article Cheng-Hao Jin, Kyu-Yeon Jun, Eunjung Lee, Seongrak Kim, Youngjoo Kwon, Kunhong Kim, Younghwa Na Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-11-19 13:04:06
¶ªÊ§µÄС¹ÇÍ·
½ð³æ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 940
- ºì»¨: 1
- Ìû×Ó: 25
- ÔÚÏß: 10.1Сʱ
- ³æºÅ: 2357066
- ×¢²á: 2013-03-18
- ÐÔ±ð: MM
- רҵ: Ò©Îﻯѧ

3Â¥2014-11-19 14:07:46














»Ø¸´´ËÂ¥